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Pain Mechanisms of Knee Joint Osteoarthritis

Pain Mechanisms of Knee Joint Osteoarthritis
膝关节骨关节炎的疼痛机制
批准号:
9068662
负责人:
DI CHEN
金额:
$34.43万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-01 至 2018-05-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Patients suffering from persistent knee joint pain typically have cartilage degeneration with structural and morphological changes in synovium, meniscus and subchondral bone at the damage knee joint region. Osteoarthritis is a leading cause of musculoskeletal-associated pain, psychological distress, impaired quality of life, and staggering socio-economic costs (estimated at $100 billion per year in the US alone). Currently, there is no effective treatment for this common affliction. Relief of knee joint pain is hampered because causative mechanisms (e.g., the pain source and affected cellular pathways) have not yet been established. To investigate the etiology of back pain and assess opportunities for possible clinical intervention, we will investigate specific signaling pathways leading to knee joit osteoarthritis and its symptom, knee pain by using representative tools: 1) established OA animal model model for facilitating behavioral pain assessments that allow us to investigate pain mechanisms, 2) genetically modified mice to understand pathophysiological nociceptive pathway evoked by knee osteoarthritis, and 3) investigation of peripheral (dorsal root ganglions) and central (spinal dorsal horn) responses by knee joint OA and roles of glial activation in chronic knee joint osteoarthritic pain. Our studies may uncover the nociceptive pathway that is impaired in OA condition, and may reveal that alleviation of OA pain at the spinal level is indeed beneficial to the joints by arresting progressive cartilage destruction through neurogenic attenuation. Successful completion of these studies will establish that effective controls of the PKC axis not only protects peripheral knee joint tissues from further degeneration, but also relieves its clinically debilitating symptom, pain, that profoundly impacts on the quality of life or a vast number of patients.
期刊论文(2)
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会议论文
Corrigendum to "Lactoferricin enhances BMP7-stimulated anabolic pathways in intervertebral disc cells" [Gene. 2013 Jul. 25; 524(2):282-91].
“乳铁蛋白增强椎间盘细胞中 BMP7 刺激的合成代谢途径”的勘误 [Gene。
DOI: 10.1016/j.gene.2016.06.021
发表时间: 2017
期刊: Gene
影响因子: 3.5
作者: [Ellman,MichaelB, Kim,Jaesung, An,HowardS, Chen,Di, Kc,Ranjan, Li,Xin, Xiao,Guozhi, Yan,Dongyao, Suh,Joon, vanWijnen,AndreJ, Wang,JamesH-C, Kim,Su-Gwan, Im,Hee-Jeong]
通讯作者: Im,Hee-Jeong
Link N as a therapeutic agent for discogenic pain.
Link N 作为椎间盘源性疼痛的治疗剂。
DOI: 10.1002/jsp2.1008
发表时间: 2018
期刊: JOR spine
影响因子: 3.7
作者: [Noorwali,Hussain, Grant,MichaelP, Epure,LauraM, Madiraju,Padma, Sampen,Hee-Jeong, Antoniou,John, Mwale,Fackson]
通讯作者: Mwale,Fackson
The Role of MicroRNA in Osteoarthritis
  • 批准号:
    9317937
  • 项目类别:
  • 资助金额:
    $34.54万
  • 财政年份:
    2017
  • 负责人:
    DI CHEN
  • 依托单位:
Allosteric Small Molecule Inhibitor Of Nerve Growth Factor Signaling in Low Back Pain
  • 批准号:
    9146276
  • 项目类别:
  • 资助金额:
    $17.05万
  • 财政年份:
    2015
  • 负责人:
    DI CHEN
  • 依托单位:
Beta-Catenin Signaling and Pathogenesis of Osteoarthritis
  • 批准号:
    7740673
  • 项目类别:
  • 资助金额:
    $34.65万
  • 财政年份:
    2009
  • 负责人:
    DI CHEN
  • 依托单位:
Beta-Catenin Signaling and Pathogenesis of Osteoarthritis
  • 批准号:
    8091321
  • 项目类别:
  • 资助金额:
    $3.39万
  • 财政年份:
    2009
  • 负责人:
    DI CHEN
  • 依托单位:
海外基金